Does recurrent acute myocarditis (Re-AM) have a worse prognosis compared to single acute myocarditis (S-AM)?
513 patients, including 141 consecutive patients with biopsy-proven or cardiac magnetic resonance-proven recurrent acute myocarditis (Re-AM) (median age 35 [26-45] years, 77% male, median LVEF 55%) and 372 consecutive patients with single acute myocarditis (S-AM), from an international multicenter study.
Recurrent acute myocarditis (Re-AM)
Single acute myocarditis (S-AM)
Composite of all-cause mortality, heart transplant and major ventricular arrhythmiascomposite
Recurrent acute myocarditis is a distinct clinical subgroup associated with a worse prognosis and increased arrhythmic risk compared to single acute myocarditis.
BACKGROUND: Recurrence of acute myocarditis (AM) is challenging. The management and natural history of patients who experience a recurrence of AM (Re-AM) remain poorly characterized. The aim of this study is to investigate clinical characteristics and outcomes of patients with Re-AM. METHODS: In this international multicenter study, 141 consecutive patients with biopsy-proven or cardiac magnetic resonance-proven Re-AM (35 26-45 years, 77% male, median left ventricular ejection fraction 55%) were investigated and compared with 372 consecutive patients with single acute myocarditis (S-AM). The primary outcome was a composite of all-cause mortality, heart transplant and major ventricular arrhythmias. RESULTS: =0.017). A family history of cardiomyopathy, autoimmune diseases, and ring-like late gadolinium enhancement was independently associated with a higher risk of recurrent AM. CONCLUSIONS: Re-AM is a distinct clinical subgroup of AM associated with generally worse prognosis and a specific increased arrhythmic risk compared with S-AM.
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Chiara Baggio
Antonio Cannata
Alessio Gasperetti
Journal of the American Heart Association
University College London
King's College London
University of Padua
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Baggio et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69fd7e5cbfa21ec5bbf06877 — DOI: https://doi.org/10.1161/jaha.125.046767